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• Bärnthaler
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The CRONIC-PPF Faculty

Julia KARGL (former STURM)
Assoz. Prof. Priv.-Doz. Mag. rer. nat. PhD

The CCL20-dependent fibrotic niche: interactions between ATII cells, fibroblasts and immune cells

Deputy Chair of the Division of Pharmacology, Otto Loewi Research Center

Division of Pharmacology, Otto Loewi Research Centre, Medical University of Graz, Neue Stiftingtalstraße 6, 8010 Graz
Phone: +43-316-385 74105,  e-mail

WWW: Forschungsportal Med Uni Graz
ORCID: 0000-0002-0870-0816
PubMed: PubMed (nih.gov)

• Profile      • Curriculum vitae     • Publications    

Julia Kargl is an immunologist and pharmacologist. Her research focuses on the discovery of novel pro- and anti-tumorigenic mediators within the lung. The Kargl lab uses a comprehensive platform to profile the immune landscape of lung disease, specifically investigating neutrophil and T-cell function in patients and preclinical models. Within the CRONIC-PPF project, she provides expertise in immune phenotyping and myeloid cell signaling.

Project

The CCL20-dependent fibrotic niche: interactions between ATII cells, fibroblasts and immune cells
Co-PI: Izabela Borek

Research interests

  1. Decoding immune cell phenotypes and functional heterogeneity in cancer and COPD: My research identifies how chronic inflammatory conditions, such as COPD and cancer, reprogram the immune landscape to influence both disease progression and therapeutic response. (Busch et al., 2016 [↗]; Kargl et al., 2017 [↗]; Mark et al., 2018 [↗]; Veatch et al., 2018 [↗]; Lastwika et al., 2019 [↗]; Kargl et al., 2019 [↗]; Valadez-Cosmes et al., 2021 [↗]; Kienzl et al., 2021 [↗]; Zhang et al., 2022 [↗])
  2. Mechanistic role of neutrophil-derived enzymes in lung cancer growth and fibrosis: Moving beyond cellular enumeration, my work focuses on how neutrophil-secreted enzymes like myeloperoxidase (MPO) and neutrophil elastase act as local signaling modulators that promote tumor survival and tissue remodeling. (Gregory et al., 2015 [↗]; Metz et al., 2016 [↗]; Valadez-Cosmes et al., 2023 [↗]; Cosic-Mujkanovic et al., 2023 [↗])
  3. Inflammatory dysregulation and innate–adaptive crosstalk in early pregnancy: This research examines how tightly regulated inflammation is required for a successful pregnancy. It explores mechanisms of dysregulation in gestational diabetes mellitus (GDM) and recurrent pregnancy loss, with a focus on the role of maternal neutrophils and myeloid enzymes at the feto–maternal interface. (Gorsek Sparovec et al., 2022 [↗]; Kuentzel et al., 2022 [↗]; Vondra et al., 2023 [↗]; Mihalic et al., 2023a [↗]; Mihalic et al., 2023b [↗])